ANVISA registration
Família HemosIL FDP
Registration 80003610521. PRODUTO DE DEGRADAÇÃO DE FIBRINOGÊNIO/ FIBRINA (FDP)
Registration details
| Registration number | 80003610521 |
|---|---|
| Application number | 25351048756201701 |
| Technical name | PRODUTO DE DEGRADAÇÃO DE FIBRINOGÊNIO/ FIBRINA (FDP) |
| Risk class | II |
| Published on | 02/05/2017 |
| Validity | Indefinite validity |
Registration holder
| Legal name | WERFEN MEDICAL LTDA |
|---|---|
| CNPJ | 02.004.662/0001-65 |
Manufacturing sites
- BIOKIT S/A ESPANHA
- BIOKIT SA ESPANHA
Other registrations held by WERFEN MEDICAL LTDAview all
IL TESTE EMULSAO DE REFERENCIA
80003610043HEMOSIL APTT-SP
80003610045ENSAIO DE CONTROLE NORMAL DE HEMOSIL
80003610048IL TESTE PLASMA REAGENTE FATOR V RESISTENCIA DOFATOR V a APC
80003610051FAMILIA DE CONTROLES UNI OU MULTIPARÂMETROS-HEMOSIL ENSAIO DE CONTROLE ANORMAL ALTO E BAIXO - WERFEN
80003610113GEM CVP
80003610117Source: ANVISA open data, medical device file, updated daily. The public database provides registration validity, rather than registration status: this registration may have been cancelled before its expiry date without this being shown here. Before making purchasing, import or marketing decisions, check the ANVISA search portal.
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